A Novel Homozygous KLHL3 Mutation as a Cause of Autosomal Recessive Pseudohypoaldosteronism Type II Diagnosed Late in Life

por Etges, Annika, Hellmig, Nicole, Walenda, Gudrun, Haddad, Bassam G., Machtens, Jan-Philipp, Morosan, Thomas, Rump, Lars Christian, Scholl, Ute I.
Publicado 2022